Improved quantum yield in geometrically constrained tetraphenylethylene-based metalorganic frameworks

被引:2
作者
Stawiasz, Katherine J. [1 ,2 ]
Deneff, Jacob I. [3 ]
Reyes, Raphael A. [3 ]
Woods, Toby J. [6 ,7 ]
Rohwer, Lauren E. S. [4 ]
Valdez, Nichole [5 ]
Rodriguez, Mark A. [5 ]
Lawal, Abdul [2 ]
Moore, Jeffrey S. [1 ,2 ]
Gallis, Dorina F. Sava [3 ]
机构
[1] Univ Illinois, Beckman Inst Adv Sci & Technol, Urbana, IL 61801 USA
[2] Univ Illinois, Dept Chem, Urbana, IL 61801 USA
[3] Sandia Natl Labs, Nanoscale Sci Dept, Albuquerque, NM 87185 USA
[4] Sandia Natl Labs, Adv Packaging Integrat Dept, Albuquerque, NM 87185 USA
[5] Sandia Natl Labs, Mat Characterizat & Performance Dept, Albuquerque, NM 87185 USA
[6] Univ Illinois, George L Clark Xray Facil, Urbana, IL 61801 USA
[7] Univ Illinois, 3M Mat Lab, Urbana, IL 61801 USA
关键词
METAL-ORGANIC FRAMEWORKS; DESIGN;
D O I
10.1039/d3ce00228d
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Herein, we report the synthesis of a novel, tetraphenylethylenebased ligand for metal-organic frameworks (MOFs). Incorporation of this ligand into a Zn- or Eu-based MOF increased the quantum yield (QY) by almost 2.5x compared to the linker alone. Furthermore, the choice of guest solvent impacted the QY and solvatochromatic response. These shifts are consistent with solvent dielectric constant as well as molecular polarizability.
引用
收藏
页码:2701 / 2705
页数:5
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